I've been diagnosed

Start with what happens next

A diagnosis is a lot to take in. You do not need to understand everything today. Here is the shape of the journey, so you can start where you want to start.

Reason for hope

Found early and treated, breast cancer has a high chance of recovery. A team of specialists will guide each step with you.

Your care team

Breast cancer is treated by a multidisciplinary team, so several specialists plan your care together.

Each person on that team is an expert in their own field. You are the expert on you. Your questions, your worries and what matters to you belong in the plan, so say them out loud.

A surgeon and a cancer doctor (oncologist)

A radiologist and a radiographer for scans and radiation

A pathologist who examines the tissue

A specialist nurse, and a reconstructive surgeon if needed

Physiotherapy, dietetics, and psychology support

You can ask for a second opinion

Asking another doctor to look at your diagnosis is normal, and you are allowed to do it. It can confirm what you have been told, or it can open up other treatment options to talk through with your own doctor.

Questions to ask your doctor

Take these with you, and write the answers down.

  • What type of breast cancer do I have, and what stage is it?
  • What are my treatment options?
  • Can I have a second opinion?
  • What side effects should I expect, and how are they managed?
  • Where can I get support for how I am feeling?

Types of breast cancer

There are several types. Your team will tell you which one you have, which guides treatment.

DCIS

Ductal carcinoma in situ. Abnormal cells are still contained inside a milk duct and have not spread. It is non-invasive.

LCIS

Lobular carcinoma in situ. Abnormal cells inside a lobule. It is not cancer itself, but it is a sign of higher risk, so it is watched closely.

Invasive ductal

Cells that started in a milk duct have grown into nearby breast tissue. This is the most common type.

Invasive lobular

Cancer that started in the milk-producing lobules and spread into nearby tissue. The second most common type.

Hormone-receptor positive

The cells grow in response to the hormones oestrogen or progesterone. This is the most common group, about 7 in every 10 breast cancers, and hormone therapy can work against it.

HER2 positive

The cells make too much of a protein called HER2, which makes them grow faster. This is about 15 to 20 out of every 100 breast cancers. It can move more quickly if it is not treated, and targeted medicines are aimed at this protein.

Newer tests can now pick up a smaller amount of HER2, called HER2-low. It matters because it can open up targeted treatments that were not an option before.

Triple negative

The cells do not carry oestrogen, progesterone or HER2 receptors, which is where the name comes from. This is about 10 to 15 out of every 100 breast cancers. Because there is no receptor to aim at, it is treated differently and there are fewer targeted options.

Inflammatory

A less common form that often affects the skin of the breast and may not form a clear lump.

Less common types

Paget disease of the nipple and phyllodes tumours are rare. Detailed guides for these are coming.

Types are also grouped by what drives them: hormone-receptor positive, HER2 positive, or triple negative.

Special situations

Breast cancer can affect some groups differently. Fuller guides for each are coming.

Breast cancer in men

Men have a small amount of breast tissue and can get breast cancer too, though it is rare. Any lump or change behind the nipple should be checked.

Younger women

Breast cancer is less common before 40, but it does happen and can grow faster. Knowing your normal and acting on changes matters at any age.

During pregnancy

Breast cancer is rare during pregnancy and can still be treated. A care team plans treatment to protect both mother and baby. A fuller guide is coming.

How it is diagnosed

Diagnosis usually moves through these steps.

  1. Clinical breast examination

    A doctor or nurse feels both breasts and the armpits for any lump or change.

  2. Mammogram and ultrasound

    A mammogram is a low-dose breast x-ray. An ultrasound uses sound waves and can show whether a lump is solid or a fluid-filled cyst.

  3. Biopsy

    A small sample of tissue or cells is taken and examined under a microscope. For most breast cancers, a biopsy is the only way to be sure.

  4. Further tests

    An MRI, blood tests, or genetic and biomarker tests may be done to plan the right treatment.

Understanding your results

Your results describe the cancer so the team can match treatment to it.

Grade

How much the cells look like normal cells. Grade 1 cells look near-normal and grow slowly. Grade 3 cells look abnormal and can grow faster.

Tumour

Its size, where it is, and how many tumours there are.

Lymph nodes

Whether cancer has reached the lymph nodes (node-positive) or not (node-negative).

Receptors (ER, PR, HER2)

Your cells are tested for two hormone receptors, oestrogen (ER) and progesterone (PR), and for a protein called HER2. These three decide the type of breast cancer you have and which treatments will work, so this is one of the most important parts of your result.

Stages, from 0 to 4

The stage describes how far the cancer has spread.

  1. Stage 0

    Still in its place of origin and not spread to nearby tissue (in situ).

  2. Stage 1

    Small and only in the breast, not spread.

  3. Stage 2

    Larger, but not spread beyond the breast and nearby nodes.

  4. Stage 3

    Larger and may have reached surrounding tissue or lymph nodes.

  5. Stage 4

    Spread to distant parts of the body. This is also called metastatic. See living with advanced cancer.

You may also hear the TNM system, which scores the tumour (T), the lymph nodes (N), and any spread or metastasis (M).

Treatment options

Most people have a combination, planned by the team for their type and stage.

Local treatment (the breast itself)

Surgery, breast-conserving

Removing the tumour and a little surrounding tissue, such as a lumpectomy or wide local excision.

Surgery, mastectomy

Removing all the breast tissue, sometimes with lymph nodes. Reconstruction may be an option.

Radiotherapy

Targeted radiation to kill cancer cells or stop them growing, while sparing healthy tissue as much as possible.

Systemic treatment (the whole body)

Chemotherapy

Medicines that kill cancer cells or stop them dividing.

Hormone therapy

Used for cancers that are sensitive to oestrogen or progesterone.

Targeted therapy

Newer medicines that work differently from chemotherapy, aimed at specific features of the cancer.

Immunotherapy may be used in some cases. Detailed, reviewed guidance is being added.

Managing side effects

Knowing what to expect, and that side effects can be managed, is one of the most valued parts of this journey.

Treatment brings side effects, and most of them can be managed. Tell your team about anything you notice, even if it feels small or silly.

Common ones are: tiredness that rest does not fix, pain, hair and skin changes, going into menopause early, trouble with memory and concentration (often called chemo brain), and effects on your bones and heart that your team will watch.

None of this is something you have to put up with quietly. There is almost always something that helps.

Newly diagnosed? You are not alone.

CANSA's toll-free help line can talk you through what is next, in your own language.

0800 22 66 22

How we made this page

  • Early draft, June 2026
  • Clinical review: pending
  • Audio in isiXhosa, isiZulu & Afrikaans planned
Where this information comes from

Facts and definitions on this page are stated in our own words from the sources above. This is an early draft for awareness only and is not medical advice. Always follow the guidance of your own care team.